Please answer all 3 questions. Using cyclopentanone as the reactant, show the product of the indicated...
please answer all of the following questions.
02 pts.] Briefly explain why the following reaction yields the Hofmann product exclusively even though the base is not sterically hindered: This is breause Br is a jood Ieavng Br CH,CH2ONa oup on q dcarloon. CH,CH,он [02 pts.] Draw the structure of alkyl that will undergo an E2 elimination to yield only the indicated alkene. CHyCHONa CHсH,он [04 pts.] Draw only the major product for each of the following elimination reactions. сн-сH,ON CнH-CHон...
Please see online the molecular wheights if needed
please answer all questions throughly
density of acetic anhydride is 1.08
Report the melting point range of aspirin and compare it to the literature value in a t format 2. able 3a. Calculate the moles of aspirin that salicylic acid would form if it were the limiting reactant. Use proper significant figures, units and show all work. 3b. Calculate the moles of aspirin that acetic anhydride would form if it were the...
Can
you check my answers please?
To answer the questions below use the following information: Cyanohydrins are important intermediates in the synthesis of c-hydroxycarboxylic acids from ketones and aldehydes. The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid. Nitriles can also be hydrolyzed to carboxylic acids using aqueous base. Unfortunately, when a cyanohydrin is treated with aqueous base the original carbonyl compound is isolated OH CHCOOH HO CN OBU H HCEN H NAOH H20...
acid catalyzed hydration of 1 methylcyclohexene yields 2
alcohols. The major product does not undergo oxidation, while the
minor product will undergo oxidation, explain.
3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol. 5. Identify the reagents you would use to accomplish each of the following transformations: DH (4) tage...
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol Show a mechanism for this reaction. 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol
Show the product of reaction of the indicated ester with LDA,
followed by butyl iodide.
CHÚCH 0 1. Provide a correct name for the indicated ester. 2. How many signals would we expect to see in the 13C NMR spectrum? 3. Show the combination of reagents required to synthesize the indicated structure using a Fischer esterification reaction. 4. a. The indicated ester is submitted to Claisen condensation conditions, using the appropriate alkoxide base and a second acidification step. The product...
Please answer all questions and show all work 1. Write a mechanism for the acid-catalyzed esterification that uses cyclopentanol and acetic acid. 2. Tertiary alcohols do not work well in the procedure outlined for this experiment; they give a different product from what you might expect. Explain this and draw the expected product from t-butyl alcohol (2-methyl-2-propanol).
Can you please answer all of the following questions. There
are 2 pictures attached. Please help
4. al Reaction Calculations (Fill in the blanks) (3 points): aldehydeNORVEEOHacensation product MW or Conc volume density mass 2 M/ 9596 3 mL/4 mL 0.75 mL Theoretical Yield mmol Yield 1.0 equivalents "You will be assigned one of three aldehydes and one of three ketones by your TA b) What is the theoretical yield of aldol product that can form using the amounts of...
HW 22: Enolates 1. Provide a detailed, stepwise mechanism for the base-catalyzed enolization (keto enol tautomerism) of acetaldehyde. 2. Provide the major organic product of the folowing reaction. 3. Provide the major organic product of the following reaction LDA 4. Which of the following ketones will give a positive iodoform test? A) 4-heptanone D) cyclohexanone B) 3-hexanone C)2-hexanone 5. Provide the major organic product of the following reaction. 6. Provide the structure of the major organic product which results when...
Please answer this question and show each major organic
product. Show all work. Thanks.
Draw the skeletal structure of the indicated major organic product synthesized from this reaction sequence (this is NOT asking you to draw the by-product, but the product with the most carbons). The answer key will be shown once you have exhausted your submissions for a particular part. 1. NaOCHCHMOP A 2. aq acid NaOH heat MOP B 1. aq acid 2. heat MOPC